Melanoma on skull
REGISTER
The information on this site is not intended or implied to be a substitute for professional medical advice, diagnosis or treatment. Content within the patient forum is user-generated and has not been reviewed by medical professionals. Other sections of the Melanoma Research Foundation website include information that has been reviewed by medical professionals as appropriate. All medical decisions should be made in consultation with your doctor or other qualified medical professional.

Melanoma on skull

› Forums › General Melanoma Community › Melanoma on skull

  • Post
    • March 8, 2014 at 7:49 pm
    nancyg
    Participant

    Can Melanoma that spread to the skull spread to the brain?   It has not happened yet…thank God… Had a brain MRI… Last Friday… Results negative (Soo happy).. Dr. said chances are slim of it spreading to brain???Hoping that is true,but not believing it.

    On a side note, dr described my husband's response to ipi as "mixed"…. He had considerable shrinkage in his chest and tumor on lung…. But PET and Bone scan show three new tumors…. So we are thrilled about the shrinkage, but again worried…. They are trying to get the insurance to approve another round of ipi…the battle of this beast continues..

    Any input you have would be appreciated!

    Thanks and God Bless you all

    Nancy 

     

Viewing 11 reply threads
  • Replies
      • March 8, 2014 at 9:06 pm
      Gene_S
      Participant

      Hello Nancy,

      My husband first lesion was on the skull as well as the second, third and fifth and he never had any brain mets but became stage IV with lesions in the lungs and liver.

      His first surgery was in January 2008.  You can read more in his profile if you desire.

      Judy (loving wife of Gene Stage IV and now NED since Oct. 2012)

        • November 3, 2017 at 3:49 pm
        scmccann
        Participant

        Dear Judy, My husband was diagnosed with Stage IV melanoma in 2012. I would love to hear how your husband got to be NED.

        Sandra (loving wife of Jim)

      • March 8, 2014 at 9:06 pm
      Gene_S
      Participant

      Hello Nancy,

      My husband first lesion was on the skull as well as the second, third and fifth and he never had any brain mets but became stage IV with lesions in the lungs and liver.

      His first surgery was in January 2008.  You can read more in his profile if you desire.

      Judy (loving wife of Gene Stage IV and now NED since Oct. 2012)

      • March 8, 2014 at 9:06 pm
      Gene_S
      Participant

      Hello Nancy,

      My husband first lesion was on the skull as well as the second, third and fifth and he never had any brain mets but became stage IV with lesions in the lungs and liver.

      His first surgery was in January 2008.  You can read more in his profile if you desire.

      Judy (loving wife of Gene Stage IV and now NED since Oct. 2012)

      • March 9, 2014 at 3:02 am
      JerryfromFauq
      Participant

      Haven't seen any statistics on this question, but would not expect it be be higher than the 40-50% chance that at the stage Iv level it can go to the brain for any of us.

      • March 9, 2014 at 3:02 am
      JerryfromFauq
      Participant

      Haven't seen any statistics on this question, but would not expect it be be higher than the 40-50% chance that at the stage Iv level it can go to the brain for any of us.

      • March 9, 2014 at 3:02 am
      JerryfromFauq
      Participant

      Haven't seen any statistics on this question, but would not expect it be be higher than the 40-50% chance that at the stage Iv level it can go to the brain for any of us.

      • March 9, 2014 at 4:02 pm
      arthurjedi007
      Participant

      I assume by skull you mean the skull bones. Based on a PET in October mine spread to the back skull bone and later on a PET in early February to the top left and right skull bone areas.

      The Dr was suprised the MRI in mid February showed no brain mets yet. Actually I believe he's still suprised all mine are still in lots of bones but nowhere else yet.

      So yes mel can go anywhere but at least you are getting some response from ipi so that is great.

       

      • March 9, 2014 at 4:02 pm
      arthurjedi007
      Participant

      I assume by skull you mean the skull bones. Based on a PET in October mine spread to the back skull bone and later on a PET in early February to the top left and right skull bone areas.

      The Dr was suprised the MRI in mid February showed no brain mets yet. Actually I believe he's still suprised all mine are still in lots of bones but nowhere else yet.

      So yes mel can go anywhere but at least you are getting some response from ipi so that is great.

       

      • March 9, 2014 at 4:02 pm
      arthurjedi007
      Participant

      I assume by skull you mean the skull bones. Based on a PET in October mine spread to the back skull bone and later on a PET in early February to the top left and right skull bone areas.

      The Dr was suprised the MRI in mid February showed no brain mets yet. Actually I believe he's still suprised all mine are still in lots of bones but nowhere else yet.

      So yes mel can go anywhere but at least you are getting some response from ipi so that is great.

       

      • March 10, 2014 at 12:09 am
      nancyg
      Participant

      Thanks everyone for your responses

      • March 10, 2014 at 12:09 am
      nancyg
      Participant

      Thanks everyone for your responses

      • March 10, 2014 at 12:09 am
      nancyg
      Participant

      Thanks everyone for your responses

Viewing 11 reply threads
  • You must be logged in to reply to this topic.
About the MRF Patient Forum

The MRF Patient Forum is the oldest and largest online community of people affected by melanoma. It is designed to provide peer support and information to caregivers, patients, family and friends. There is no better place to discuss different parts of your journey with this cancer and find the friends and support resources to make that journey more bearable.

The information on the forum is open and accessible to everyone. To add a new topic or to post a reply, you must be a registered user. Please note that you will be able to post both topics and replies anonymously even though you are logged in. All posts must abide by MRF posting policies.

Popular Topics